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2,4-dichloro-3-methylbenzenesulfonyl chloride(SALTDATA: FREE) is a chemical compound with the molecular formula C7H6Cl2O2S and a molar mass of 235.1 g/mol. It is a white to light yellow solid and is commonly used as a sulfonylating agent in organic synthesis.
Used in Pharmaceutical Industry:
2,4-dichloro-3-methylbenzenesulfonyl chloride(SALTDATA: FREE) is used as a reagent in the synthesis of pharmaceuticals for its high reactivity, enabling the production of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 2,4-dichloro-3-methylbenzenesulfonyl chloride(SALTDATA: FREE) is utilized as a reagent in the synthesis of agrochemicals, contributing to the development of effective products for agricultural applications.
Used in Dye Production:
2,4-dichloro-3-methylbenzenesulfonyl chloride(SALTDATA: FREE) is also used in the production of dyes, where its reactivity aids in creating a range of colorants for various industries.
Used in Organic Compound Synthesis:
2,4-dichloro-3-methylbenzenesulfonyl chloride(SALTDATA: FREE) is employed in the synthesis of other organic compounds, showcasing its versatility as a sulfonylating agent in organic chemistry.
Safety Precautions:
Due to its strong irritant properties, 2,4-dichloro-3-methylbenzenesulfonyl chloride(SALTDATA: FREE) should be handled with care to avoid skin, eye, and respiratory system irritation. It should be stored in a cool, dry place away from sources of ignition to ensure safety.

69145-58-0

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69145-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69145-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,4 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69145-58:
(7*6)+(6*9)+(5*1)+(4*4)+(3*5)+(2*5)+(1*8)=150
150 % 10 = 0
So 69145-58-0 is a valid CAS Registry Number.

69145-58-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dichloro-3-methylbenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 2,6-Dichlor-toluol-3-sulfonylchlorid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69145-58-0 SDS

69145-58-0Upstream product

69145-58-0Downstream Products

69145-58-0Relevant academic research and scientific papers

Design and synthesis of novel sulfonamide-containing bradykinin hB 2 receptor antagonists. 1. Synthesis and SAR of α,α- dimethylglycine sulfonamides

Fattori, Daniela,Rossi, Cristina,Fincham, Christopher I.,Berettoni, Marco,Calvani, Federico,Catrambone, Fernando,Felicetti, Patrizia,Gensini, Martina,Terracciano, Rosa,Altamura, Maria,Bressan, Alessandro,Giuliani, Sandro,Maggi, Carlo A.,Meini, Stefania,Valenti, Claudio,Quartara, Laura

, p. 3602 - 3613 (2007/10/03)

We recently published the extensive in vivo pharmacological characterization of MEN 16132 (J. Pharmacol. Exp. Ther. 2005, 616-623; Eur. J. Pharmacol. 2005, 528, 7), a member of the sulfonamide-containing human B 2 receptor (hB2R) ant

NON-PEPTIDE BRADYKININ ANTAGONISTS AND PHARMACEUTICAL COMPOSITIONS THEREFROM

-

Page/Page column 9, (2010/11/08)

Non-peptide compounds having activity as selective antagonists of bradykinin (BK) B2 receptor. The compounds are chemically characterized by the presence of an amino acid alpha substituted with a cyclic group and by a tetraalkylammonium group.

Sulfonyl chloride as a disposable electron withdrawing substituent in halex fluorinations

Kageyama, Hiroyuki,Suzuki, Hiroshi,Kimura, Yoshikazu

, p. 85 - 89 (2007/10/03)

Syntheses of 1,3-difluorobenzene and 2,6-difluorotoluene are described via chlorosulfonation, catalytic Halex-fluorination, and desulfination of 1,3-dichlorobenzene and 2,6-dichlorotoluene.

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